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Plasmid
Why do we sometimes obtain a lower yield?
Why doesn't the eluted DNA perform well in downstream applications?
Can the plasmid DNA extraction Kit be applied on Gram (+) bacteria?
Why do we get eluted plasmid contaminated with RNA?
Why can't the eluted plasmid be cut by restriction enzymes properly?
Why does the Plasmid DNA Extraction Kit require two washings with two types of wash buffers (W1 and Wash Buffer) while competitors kits require one washing?
Eluted plasmid appeared degraded after storage for an extended period of time.
Why was Restriction enzyme digestion unsuccessful?
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